Package 42291-510-01

Brand: primaquine phosphate

Generic: primaquine phosphate
NDC Package

Package Facts

Identity

Package NDC 42291-510-01
Digits Only 4229151001
Product NDC 42291-510
Description

100 TABLET, FILM COATED in 1 BOTTLE (42291-510-01)

Marketing

Marketing Status
Marketed Since 2019-02-21
Brand primaquine phosphate
Generic primaquine phosphate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4ba945a5-47a2-e791-e063-6294a90a9f8a", "openfda": {"unii": ["H0982HF78B"], "rxcui": ["904170"], "spl_set_id": ["82465385-4602-7f46-e053-2991aa0a9fdf"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (42291-510-01)", "package_ndc": "42291-510-01", "marketing_start_date": "20190221"}], "brand_name": "PRIMAQUINE PHOSPHATE", "product_id": "42291-510_4ba945a5-47a2-e791-e063-6294a90a9f8a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimalarial [EPC]"], "product_ndc": "42291-510", "generic_name": "PRIMAQUINE PHOSPHATE", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PRIMAQUINE PHOSPHATE", "active_ingredients": [{"name": "PRIMAQUINE PHOSPHATE", "strength": "15 mg/1"}], "application_number": "ANDA206043", "marketing_category": "ANDA", "marketing_start_date": "20190221", "listing_expiration_date": "20271231"}